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2
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本文引用的文献

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Mitosis-specific phosphorylation of histone H3 initiates primarily within pericentromeric heterochromatin during G2 and spreads in an ordered fashion coincident with mitotic chromosome condensation.组蛋白H3的有丝分裂特异性磷酸化主要在G2期的着丝粒周围异染色质内起始,并以有序的方式扩展,与有丝分裂染色体凝聚同步。
Chromosoma. 1997 Nov;106(6):348-60. doi: 10.1007/s004120050256.
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Condensins, cohesins, and chromosome architecture: how to make and break a mitotic chromosome.凝聚素、黏连蛋白与染色体结构:如何构建与拆解有丝分裂染色体
Cell. 1997 Oct 3;91(1):5-8. doi: 10.1016/s0092-8674(01)80002-7.
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Crystal structure of the nucleosome core particle at 2.8 A resolution.核小体核心颗粒的晶体结构,分辨率为2.8埃。
Nature. 1997 Sep 18;389(6648):251-60. doi: 10.1038/38444.
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Mitotic chromosome condensation.有丝分裂染色体凝聚
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5
Vanadate triggers the transition from chromosome condensation to decondensation in a mitotic mutant (tsTM13) inactivation of p34cdc2/H1 kinase and dephosphorylation of mitosis-specific histone H3.钒酸盐在有丝分裂突变体(tsTM13)中引发从染色体凝聚到解凝聚的转变,使p34cdc2/H1激酶失活并使有丝分裂特异性组蛋白H3去磷酸化。
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Alteration of cell cycle-dependent histone phosphorylations by okadaic acid. Induction of mitosis-specific H3 phosphorylation and chromatin condensation in mammalian interphase cells.冈田酸对细胞周期依赖性组蛋白磷酸化的改变。在哺乳动物间期细胞中诱导有丝分裂特异性H3磷酸化和染色质凝聚。
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Chromosome condensation in Xenopus mitotic extracts without histone H1.非洲爪蟾有丝分裂提取物中无组蛋白H1时的染色体凝聚
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8
Mitogen-stimulated phosphorylation of histone H3 is targeted to a small hyperacetylation-sensitive fraction.有丝分裂原刺激的组蛋白H3磷酸化作用针对一小部分对超乙酰化敏感的区域。
Proc Natl Acad Sci U S A. 1994 May 24;91(11):4781-5. doi: 10.1073/pnas.91.11.4781.
9
A heterodimeric coiled-coil protein required for mitotic chromosome condensation in vitro.一种体外有丝分裂染色体凝聚所需的异源二聚体卷曲螺旋蛋白。
Cell. 1994 Nov 4;79(3):449-58. doi: 10.1016/0092-8674(94)90254-2.
10
Chromosome condensation induced by fostriecin does not require p34cdc2 kinase activity and histone H1 hyperphosphorylation, but is associated with enhanced histone H2A and H3 phosphorylation.福司曲星诱导的染色体凝聚不需要p34cdc2激酶活性和组蛋白H1的过度磷酸化,但与组蛋白H2A和H3磷酸化增强有关。
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在四膜虫的有丝分裂和减数分裂过程中,组蛋白H3丝氨酸10位点的磷酸化与染色体浓缩相关。

Phosphorylation of histone H3 at serine 10 is correlated with chromosome condensation during mitosis and meiosis in Tetrahymena.

作者信息

Wei Y, Mizzen C A, Cook R G, Gorovsky M A, Allis C D

机构信息

Department of Biology, University of Rochester, Rochester, NY 14627, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7480-4. doi: 10.1073/pnas.95.13.7480.

DOI:10.1073/pnas.95.13.7480
PMID:9636175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC22657/
Abstract

H3 phosphorylation has been correlated with mitosis temporally in mammalian cells and spatially in ciliated protozoa. In logarithmically growing Tetrahymena thermophila cells, for example, H3 phosphorylation can be detected in germline micronuclei that divide mitotically but not in somatic macronuclei that divide amitotically. Here, we demonstrate that micronuclear H3 phosphorylation occurs at a single site (Ser-10) in the amino-terminal domain of histone H3, the same site phosphorylated during mitosis in mammalian cells. Using an antibody specific for Ser-10 phosphorylated H3, we show that, in Tetrahymena, this modification is correlated with mitotic and meiotic divisions of micronuclei in a fashion that closely coincides with chromosome condensation. Our data suggest that H3 phosphorylation at Ser-10 is a highly conserved event among eukaryotes and is likely involved in both mitotic and meiotic chromosome condensation.

摘要

在哺乳动物细胞中,H3磷酸化在时间上与有丝分裂相关,在纤毛原生动物中与空间相关。例如,在对数生长期的嗜热四膜虫细胞中,可在进行有丝分裂的生殖系微核中检测到H3磷酸化,而在进行无丝分裂的体细胞大核中则检测不到。在此,我们证明微核H3磷酸化发生在组蛋白H3氨基末端结构域的单个位点(Ser-10),这与哺乳动物细胞有丝分裂期间磷酸化的位点相同。使用针对Ser-10磷酸化H3的特异性抗体,我们表明,在四膜虫中,这种修饰与微核的有丝分裂和减数分裂相关,其方式与染色体浓缩密切一致。我们的数据表明,Ser-10处的H3磷酸化在真核生物中是一个高度保守的事件,可能参与有丝分裂和减数分裂的染色体浓缩。